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SCN5A Variant P1962S

Summary of observed carriers, functional annotations, and structural context for SCN5A P1962S. Data combine curated literature, international cohorts, and gnomAD observations.

Estimated LQT3 penetrance

3%

0/11 effective observations

Estimated BrS1 penetrance

6%

0/11 effective observations

Total carriers

1

0 BrS1 · 0 LQT3 · 1 unaffected

P1962S is present in 1 alleles in gnomAD. This residue resides in a Non_Hotspot region for Brugada syndrome and a Non_Hotspot region for LQT3.

Variant features alone are equivalent to phenotyping 0 individuals for Brugada syndrome and 0 individuals for LQT3.

In silico predictors

Variant-level computational predictors.
PROVEAN PolyPhen-2 BLAST-PSSM REVEL Penetrance Density BrS (%) Penetrance Density LQT3 (%)
-1.52 0.022 0.61 0.343 0 0

PROVEAN scores below -2 suggest deleterious impact. REVEL scores above 0.5–0.75 are often interpreted as likely pathogenic. PolyPhen-2 scores above 0.85 are typically pathogenic. Penetrance density summarises neighbouring residue risk (Kroncke et al. 2019).

Reported carrier data

Observed carriers by publication or cohort.
Source Year Carriers Unaffected LQT3 BrS1 Other Other Disease
29907895 2018 2 0 0 2 SIDS
Literature, cohort, and gnomAD 1 1 0 0
Variant features alone 15 15 0 0

Totals may differ from individual publications due to duplicate patients removed during curation.

Functional data

Peak and late/persistent current values are relative to wild-type (100% indicates no change). V1/2 activation and inactivation denote the membrane potentials (mV) at which half-maximal current is achieved.

Published electrophysiology measurements.
PubMed ID Year Cell Type Peak Current (% WT) V1/2 Activation (mV) V1/2 Inactivation (mV) Late/Persistent Current (% WT)
29907895 2018

Nearby variants

Neighbouring residues within 15 Ångström provide structural context. Variants listed in the right-most column have been observed clinically or in gnomAD.

Previously observed variants near P1962S.
Neighbour residue Distance (Å) Observed variants
1947 15
1948 14 I1948V,
1949 14 A1949S, A1949T,
1950 13 Y1950C,
1951 13 V1951L, V1951M,
1952 12
1953 11 p.S1953RfsX84,
1954 11 E1954K,
1955 10 N1955Y,
1956 9
1957 8 S1957P,
1958 8 R1958Q, R1958P, R1958X,
1959 7
1960 5
1961 4
1962 0 P1962S, P1962L
1963 4 P1963L,
1964 5 S1964F,
1965 7 S1965G, S1965N,
1966 8
1967 8 p.S1967LfsX12,
1968 9 I1968N, I1968T, I1968S, I1968V, I1968M,
1969 10
1970 11 p.S1970_S1972del,
1971 11
1972 12
1973 13 F1973L,
1974 13
1975 14 P1975T,
1976 14 S1976C,
1977 15 Y1977N,